George Clinical’s medical monitors come from diverse therapeutic backgrounds, and have the clinical and research expertise required to provide rigorous medical oversight of clinical trials. According to the needs of the trial, our medical monitors are able to provide a number of services, such as:

• Providing input into the study protocol, informed consent forms, project risk assessment
• Training investigational sites and study teams
• Supporting investigational sites with queries around eligibility, safety etc.
• Reviewing SAEs, coding of SAEs and writing safety narratives
• Reviewing patient data to identify trends and risks across the study

George Clinical’s medical monitors are regionally located to provide complete coverage for investigational sites in various time zones. In addition, appointment of local medical monitors provides the added benefit of communication in the local language, and a familiarity with local clinical practices and culture, which in-turn, helps to foster stronger ties with investigational sites and study teams.

George Clinical’s medical monitors provide rigorous medical oversight from design throughout delivery.

Medical monitors provide rigorous medical oversight from design to delivery.